Binding specificity of protein phosphatase 2A core enzyme for regulatory B subunits and T antigens

J Virol. 1999 Jan;73(1):839-42. doi: 10.1128/JVI.73.1.839-842.1999.

Abstract

The core enzyme of protein phosphatase 2A is composed of a regulatory subunit A and a catalytic subunit C. It is controlled by three types of regulatory B subunits (B, B', and B") and by tumor (T) antigens, which are unrelated by sequence but bind to overlapping regions on the A subunit. To find out whether the different B subunits and T antigens bind to identical or distinct amino acids of the A subunit, mutants were generated and their abilities to bind B subunits and T antigens were tested. We found that some amino acids are involved in the binding of all types of B subunits, whereas others are specifically involved in the binding of one or two types of B subunits. T-antigen-binding specificity does not correlate with that of a particular type of B subunit.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Antigens, Polyomavirus Transforming / chemistry*
  • Antigens, Polyomavirus Transforming / metabolism
  • Binding Sites
  • Molecular Sequence Data
  • Mutation
  • Phosphoprotein Phosphatases / chemistry*
  • Phosphoprotein Phosphatases / metabolism
  • Protein Phosphatase 2

Substances

  • Antigens, Polyomavirus Transforming
  • Phosphoprotein Phosphatases
  • Protein Phosphatase 2